Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexanoic Acid | HCID 8892 | — |
| Edukt | alpha-Hydroxy-2-furanacetic acid | HCID 86860 | — |
| Edukt | Trimethylorthoacetate | HCID 21927715 | — |
| Lösungsmittel | Decalin | HCID 7044 | — |
| Produkt | HCID 20325098 | HCID 20325098 | 54% |
Reaktionsschritte
A solution of the product from step b.) (10.9 g, 64 mmol) in decalin (193 ml) was treated with trimethylorthoacetate (48.2 ml, 384 mmol) and hexanoic acid (2.0 ml). Next, the reaction mixture was fitted with a Vigreaux column and heated to 180° C. for 18 hours. Additional hexanoic acid (3×1.5 ml) aliquots of hexanoic acid were added every 2 hours for the first 6 hours of reaction time. Next, the reaction was cooled to 22° C. and extracted with MeOH providing 27 g of a crude mixture of the diester and decalin. This mixture was dissolved in MeOH (250 ml), cooled to 0° C., and treated with 2 M NaOH (150 ml). After 12 hours, the solvent was evaporated and the residue was taken up in 2 N NaOH (100 ml) and washed with ether (2×150 ml). The basic layer was acidified with 4 M HCl to pH 1 and back extracted with EtOAc (4×100 ml). The organic layer was washed with brine, dried (MgSO4) and concentrated providing 6.4 g (54%) of the above subtitle compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07718647B2 |
|---|
| Quelldatensatz | uspto-grants-2010_05 |
|---|
| ORD ID | ord-61297c5bd18f4a39b6271b6868695f01 |
|---|
| Quellennotiz | uspto-grants-2010_05 |
|---|